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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05238350
Other study ID # NevsehirU
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 7, 2015
Est. completion date November 11, 2015

Study information

Verified date August 2022
Source TC Erciyes University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Abstract Pain is the most common symptom of osteoarthritis and affects people's functional status with quality of life. This study was conducted to determine the effect of acupressure on pain, functional status, and quality of life in patients living with knee osteoarthritis. Acupressure application and follow-ups were performed by the researcher in the patient's home environment. The study was performed with 90 patients, 45 in the intervention group and 45 in the control group. Acupressure was performed two days a week for four weeks with a total of eight sessions on the ST34, ST35, ST36, SP9, SP10, GB34 acupuncture points following an acupressure practice guide prepared by the researcher. It was determined that while the Visual Analog Scale (VAS), the Western Ontario and McMaster University Osteoarthritis Index (WOMAC) scores of the intervention group were higher than those of the control group before application, they had decreased after application. It was found that all subscale mean scores of the Short-Form Health Survey (SF-36) quality of life questionnaire increased after application in the intervention group. It was concluded that acupressure has decreased pain severity and increased the functional status and quality of life of patients with knee osteoarthritis. Keywords: Osteoarthritis, pain, nursing, acupressure.


Description:

Abstract Background: Pain is the most common symptom of osteoarthritis and affects people's functional status with quality of life. Objective: This study was conducted to determine the effect of acupressure on pain, functional status, and quality of life in patients living with knee osteoarthritis. Methods/Design: The study was conducted as an experimental study with a pre-posttest and a control group. Settings: The study was conducted on patients diagnosed with knee osteoarthritis and attended the Physical Therapy and Rehabilitation Polyclinics of Nevşehir government hospital in the Central Anatolia Region of Turkey. Acupressure application and follow-ups were performed by the researcher in the patient's home environment. Participants: The study was performed with 90 patients, 45 in the intervention group and 45 in the control group. Intervention: Acupressure was performed two days a week for four weeks with a total of eight sessions on the ST34, ST35, ST36, SP9, SP10, GB34 acupuncture points following an acupressure practice guide prepared by the researcher. Measurement of efficacy: Data was collected before and after acupressure application by using a Visual Analogue Scale (VAS), the 36-Item Short-Form Health Survey (SF-36), and the Western Ontario and McMaster University Osteoarthritis Index (WOMAC).


Recruitment information / eligibility

Status Completed
Enrollment 90
Est. completion date November 11, 2015
Est. primary completion date June 11, 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 38 Years and older
Eligibility Inclusion Criteria: - 38 years old and over - Diagnosed by a doctor with knee OA according to American College of Rheumatology (ACR) criteria - had three points and over on the VAS pain scale, - had no communication problems - did not have any significant knee trauma within the last six months or an intra-articular steroid injection - did not have any infection in the lower extremities or wounds, surgery or physiotherapy within the last six months - those who accepted to participate to the study. Exclusion Criteria: - the patient is not willing to go on the study in any stage of the study and case of any adverse effect of acupressure.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Acupressure
Acupressure was performed two days a week for four weeks with a total of eight sessions on the ST34, ST35, ST36, SP9, SP10, GB34 acupuncture points following an acupressure practice guide prepared by the researcher.

Locations

Country Name City State
Turkey Nigde Omer Halisdemir University Nigde Ni?gde

Sponsors (3)

Lead Sponsor Collaborator
TC Erciyes University Pinar TEKINSOY KARTIN, Rabiye ÇIRPAN

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Pain level in visual analogue scale (VAS) Pain severity scores were determined by measuring values that were chosen on VAS by patients. The numerical scale ranges from 0 "No pain", to 10 "Worst pain imaginable", and a numerical value is given to every 1 cm range to measure pain severity. baseline, change from baseline at 4th week;
Secondary The Western Ontario and McMaster University Osteoarthritis Index (WOMAC) Osteoarthritis Index Their functional status levels were evaluated by using WOMAC Osteoarthritis Index.Every question is scored between 0 and 4 points evaluated with a five-way Likert-type scale. High scores from the index show increased pain and stiffness and dysfunction in physical function. baseline, change from baseline at 4th week;
Secondary 36-Item Short-Form Health Survey (SF-36) Their changes in quality of life levels were evaluated by using SF-36 scale.The scale gives separate scores for every sub-scale, which varies between 0 and 100 points. High scores on the subscales show good health status, while low scores show a deterioration in health baseline, change from baseline at 4th week;
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